Canonical Allele Identifier: CA382531332
Gene: ATM HGNC NCBI

Linked Data

dbSNP Id: rs28904919

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.108247060C>G , CM000673.2:g.108247060C>G GRCh38
NC_000011.9:g.108117787C>G , CM000673.1:g.108117787C>G GRCh37
NC_000011.8:g.107622997C>G NCBI36
NG_009830.1:g.29229C>G , LRG_135:g.29229C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000452508.7:c.998C>G ENSP00000388058.2:p.Ser333Cys
ENST00000713593.1:c.*469C>G ENSP00000518889.1:n.*469C>G
ENST00000278616.9:c.998C>G ENSP00000278616.4:p.Ser333Cys
ENST00000682516.1:n.1132C>G
ENST00000682956.1:n.1132C>G
ENST00000683100.1:n.3345C>G
ENST00000683174.1:n.1148C>G
ENST00000683605.1:n.493C>G
ENST00000684037.1:c.998C>G ENSP00000508245.1:p.Ser333Cys
ENST00000684061.1:n.1132C>G
ENST00000684179.1:n.967C>G
ENST00000527805.6:c.998C>G ENSP00000435747.2:p.Ser333Cys
ENST00000675595.1:c.833C>G ENSP00000502563.1:p.Ser278Cys
ENST00000675843.1:c.998C>G MANE Select ENSP00000501606.1:p.Ser333Cys
ENST00000278616.8:c.998C>G ENSP00000278616.4:p.Ser333Cys
ENST00000452508.6:c.998C>G ENSP00000388058.2:p.Ser333Cys
ENST00000527805.5:c.998C>G ENSP00000435747.1:p.Ser333Cys
NM_000051.3:c.998C>G , LRG_135t1:c.998C>G NP_000042.3:p.Ser333Cys
XM_005271561.3:c.998C>G XP_005271618.2:p.Ser333Cys
XM_005271562.3:c.998C>G XP_005271619.2:p.Ser333Cys
XM_006718843.2:c.998C>G XP_006718906.1:p.Ser333Cys
XM_011542840.1:c.998C>G XP_011541142.1:p.Ser333Cys
XM_011542841.1:c.998C>G XP_011541143.1:p.Ser333Cys
XM_011542842.1:c.833C>G XP_011541144.1:p.Ser278Cys
XM_011542843.1:c.998C>G XP_011541145.1:p.Ser333Cys
XM_011542844.1:c.-47C>G XP_011541146.1:n.-47C>G
XM_011542845.1:c.-141C>G XP_011541147.1:n.-141C>G
XM_011542846.1:c.998C>G XP_011541148.1:p.Ser333Cys
NM_001351834.1:c.998C>G NP_001338763.1:p.Ser333Cys
XM_005271562.5:c.998C>G XP_005271619.2:p.Ser333Cys
XM_006718843.4:c.998C>G XP_006718906.1:p.Ser333Cys
XM_011542840.3:c.998C>G XP_011541142.1:p.Ser333Cys
XM_011542842.3:c.833C>G XP_011541144.1:p.Ser278Cys
XM_011542843.2:c.998C>G XP_011541145.1:p.Ser333Cys
XM_011542844.3:c.-47C>G XP_011541146.1:n.-47C>G
XM_011542845.2:c.-141C>G XP_011541147.1:n.-141C>G
XM_017017789.2:c.998C>G XP_016873278.1:p.Ser333Cys
XM_017017790.2:c.998C>G XP_016873279.1:p.Ser333Cys
XM_017017791.1:c.998C>G XP_016873280.1:p.Ser333Cys
XM_017017792.2:c.998C>G XP_016873281.1:p.Ser333Cys
XR_002957150.1:n.1731C>G
NM_001351834.2:c.998C>G NP_001338763.1:p.Ser333Cys
NM_000051.4:c.998C>G MANE Select NP_000042.3:p.Ser333Cys